2-Chloro-N-(4-ethylphenyl)acetamide, with the CAS number 20172-36-5, is an organic compound characterized by its amide functional group, which is derived from acetic acid. This compound features a chloro substituent on the second carbon of the acetamide structure and an ethylphenyl group attached to the nitrogen atom. The presence of the chlorine atom contributes to its reactivity and potential applications in various chemical reactions. Typically, compounds like this may exhibit moderate solubility in organic solvents and limited solubility in water due to their hydrophobic aromatic components. The ethylphenyl group can influence the compound's biological activity, making it of interest in medicinal chemistry. Additionally, the compound may possess specific melting and boiling points, which are essential for its characterization and practical applications. Safety data sheets should be consulted for handling and storage guidelines, as the presence of chlorine may pose certain hazards. Overall, 2-chloro-N-(4-ethylphenyl)acetamide is a compound of interest in both synthetic and pharmaceutical chemistry.

2-chloro-N-(4-ethylphenyl)acetamide

20172-36-5: acetamide, 2-chloro-N-(4-ethylphenyl)-

2-Chloro-N-(4-ethyl-phenyl)-acetamide

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CAS 20172-36-5: 2-chloro-N-(4-ethylphenyl)acetamide

2-Chloro-N-(4-ethyl-phenyl)-acetamide

Ref: 10-F058144

2-Chloro-N-(4-ethylphenyl)acetamide

Ref: 3D-FC113928

Robenacoxib Impurity A

Ref: ST-EA-CP-R28001